Surya Prakash Goud Ponnam
VIDWAN ID: 215889

Dr Surya Prakash Goud Ponnam

Male Doctor of Philosophy
Assistant Professor (Grade-III) | Department of Molecular Biology and Biotechnology
Tezpur University
Assam
Expertise: Biology
9 Publications
3 Projects
157 Scopus Citations
66 CrossRef
16 Years 2 Months Total Experience
Publications
9 Total
Articles
8
Chapters
1
Activity

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Scopus Scopus
157 Citations
4 h-index
CrossRef CrossRef
66 Citations
3 h-index
Google Scholar Google Scholar

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Professional Recognition

Early career research (ECR-SERB,DST
2019
SERB,DST, Govt. of india
Overseas Associateship
2015
Department of Biotechnology, Govt. of India
Junior research Fellowsip
2004
ICMR, Govt. of India
Junior research Fellowship
2005
CSIR-HRDG, Govt. of India
Senior Research Fellowship
2006
CSIR-HRDG, Govt. of India

Community & Membership

Departmental Advisory Committee
Member
Jan 2010
Board of Studies
Member
Jan 2010
Indian Academy Of Medical Genetics
Associate Life Member (No.L/AM-030)
Jan 2014
The Indian Society of Human Genetics
Life Member (No.L/1726/2014)
Jan 2014
The Society of Biological Chemists (India)
Life Member (No.3354/2014)
Jan 2014

Personal Details

Doctor of Philosophy
2011
P K R Arts College for Women
Master of Science
2004
Acharya Nagarjuna University, Guntur
Bachelor of Science
2002
Kota University, Kota
Assistant Professor (Grade-III)
Jul 2019 – Present
Tezpur University | Department of Molecular Biology and Biotechnology
Assistant Professor (Grade-II)
Jul 2014 – Jul 2019
Tezpur University | Department of Molecular Biology and Biotechnology
Assistant Professor (Grade-I)
Jul 2010 – Jun 2014
Tezpur University | Department of Molecular Biology and Biotechnology
Biological Sciences
Biology

Related Profiles

Scholarly Work

Studies on genetic and epigenetic alternations on keratoconus patients from Assam, India
Other
Agency: Department of Bio-Technology Role: Principal Investigator
In vitro studies to investigate the therapeutic approach of editing the defective exon 3 of the human CHST6 gene associated with Macular Corneal Dystrophy through the CRISPR-Cas9 technology
Other
Agency: Department of Science and Technology Role: Principal Investigator
Diagnosis and Immunopathogenesis of Dengue Virus Infections; a longitudinal investigation into genotype diversity, diagnosis and immune response to dengue infections in Assam, Northeast India
Other
Agency: Defence Research and Development Organisation Role: Co-Principal Investigator

Molecular Genetic Analysis of Keratoconus Patients from Assam, India

University Tezpur University
Year 2022
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Scholarly Publications

A cataract-causing connexin 50 mutant is mislocalized to the ER due to loss of the fourth transmembrane domain and cytoplasmic domain

Open Access
Journal Article
FEBS Open Bio. Year: 2013. Volume: 3 , Issue: 1 , Pages: 22-29 .
Authors: Somaraju Chalasani, M.L.; Muppirala, M.; G. Ponnam, S.P.; Kannabiran, C.; Swarup, G.

Knockdown of XRCC5 and XRCC6 activity using CRISPR/Cas9 technology enhances homology-directed DNA repair at the CHST6 locus in HEK293 cells

Journal Article
Experimental Eye Research. Year: 2026. Volume: 271 .
Authors: Aparajita Baruah; Tobias Wimmer; Knut Stieger; Surya Prakash Goud Ponnam

A comprehensive molecular genetic analysis of keratoconus patients from assam, a northeastern state of India

Journal Article
European Journal of Ophthalmology. Year: 2022. Volume: 32 , Issue: 3 , Pages: 1361-1369 .
Authors: Mrigyanka Chakravarty; Surya Prakash Goud Ponnam; Narayan Bardoloi; Subhash Kumar; Prasanta Saikia

Development of a Reporter System to Explore MMEJ in the Context of Replacing Large Genomic Fragments

Open Access
Journal Article
Molecular Therapy - Nucleic Acids. Year: 2018. Volume: 11 , Pages: 407-415 .
Authors: Mert Yanik; Surya Prakash Goud Ponnam; Tobias Wimmer; Lennart Trimborn; Carina Müller; Isabel Gambert; Johanna Ginsberg; Annabella Janise; Janina Domicke; Wolfgang Wende; Birgit Lorenz; Knut Stieger

Mutational screening of Indian families with hereditary congenital cataract

Journal Article
Year: 2013. Volume: 19 , Pages: 1141-1148 .

A missense mutation in LIM2 causes autosomal recessive congenital cataract

Journal Article
Year: 2008. Volume: 14 , Pages: 1204-1208 .

Mutation of the gap junction protein alpha 8 (GJA8) gene causes autosomal recessive cataract.

Journal Article
Journal of Medical Genetics. Year: 2007. Volume: 44 , Issue: 7 , Pages: e85 .
Authors: Surya Prakash G Ponnam; Kekunnaya Ramesha; Sushma Tejwani; Balasubramanya Ramamurthy; Chitra Kannabiran

Evaluation of CRISPR-Cas9 mismatch activity using a BRET-based reporter system

Open Access
Journal Article
Microchemical Journal. Year: 2025. Volume: 208 , Pages: 112256 .
Authors: Tobias Wimmer; Anthony Lorenz; Lars Thomas Hossfeld; Surya Prakash Goud Ponnam; Lyubomyr Lytvynchuk; Knut Stieger
Showing 1 to 8 of 9 publications